DrugJul 31, 2024
GLOBAL WIDGET Hemp Bombs CBD Pain Freeze (menthol 4%), 400mg, 4 oz bottles recall — FDA D-0615-2024
Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
Class IIIFDA: OngoingGLOBAL WIDGET LLC
Latest records
Latest recalls — page 365
The newest recall records with useful source details are listed here.
DrugJul 31, 2024
Venlafaxine Hydrochloride Extended-Release Capsules, USP 37.5mg recall — FDA D-0617-2024
Failed Dissolution Specifications: Out-of-specification results observed for dissolution testing at the 8-hour and 12-hour pull intervals.
Class IIFDA: TerminatedZydus Pharmaceuticals (USA) Inc.
DrugJul 31, 2024
Washington Homeopathic Products Complete 30C/200C Homeopathic Kit, Contains: One hundred 1/2 recall — FDA D-0618-2024
Labeling: Label Mix-up: Some bottles of Ferrum Phosphoricum 200C were incorrectly labeled as Ferrum Metallicum 200C.
Class IIIFDA: TerminatedWashington Homeopathic Products, Inc.
VehicleJul 26, 2024
Hyundai Motor air bags recall — NHTSA campaign 24V561000
Hyundai Motor America (Hyundai) is recalling certain 2024 Santa Fe and Santa Fe HEV vehicles. The main floor wiring harness may chafe against the passenger-side second-row bench seat…
air bagsHyundai Motor America
Medical DeviceJul 24, 2024
Medical Depot Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury recall — FDA Z-2355-2024
The tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustain an injury
Class IIFDA: OngoingMedical Depot Inc.
Medical DeviceJul 24, 2024
Abbott Medical Proclaim 5 Elite Implantable Pulse Generator, REF 3660, Sterile EO, Rx Only recall — FDA Z-2369-2024
The duration between the implantable pulse generator reaching the elective replacement indicator threshold and end of service may be shorter than indicated in product labeling.
Class IIFDA: OngoingAbbott Medical
Medical DeviceJul 24, 2024
Baxter Healthcare Volara System. Blue Ventilator Adapter Module. Intermittent positive recall — FDA Z-2322-2024
Potential of the handset plug to disconnect from the nebulizer port on the blue ventilator adapter. The handset plug is required to ensure proper operation and ventilator gas flow.
Class IFDA: OngoingBaxter Healthcare Corporation
Medical DeviceJul 24, 2024
Waldemar Link GmbH & Co. KG Endo Model M Tibial Components Modular Knee Prosthesis System recall — FDA Z-2410-2024
Blind screws of the modular tibial component cannot be loosened intraoperatively,prolongation surgery due to intraoperatively change in procedure, probably to cementing technique
Class IIFDA: OngoingWaldemar Link GmbH & Co. KG (Mfg Site)
Medical DeviceJul 24, 2024
B. Braun Medical Infusomat SPACE PUMP IV SET, 2 CARESITES, ASV-Used with an recall — FDA Z-2387-2024
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime,…
Class IIFDA: OngoingB. Braun Medical, Inc.
Medical DeviceJul 24, 2024
B. Braun Medical Infusomat SPACE PUMP IV SET W/2 CARESITE, CKVLV -Used with an recall — FDA Z-2400-2024
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime,…
Class IIFDA: OngoingB. Braun Medical, Inc.
Medical DeviceJul 24, 2024
Medtronic Ascenda Intrathecal Catheter, Models: a) 8780 (114 cm) recall — FDA Z-2352-2024
Design update to the Ascenda Intrathecal Catheter Models 8780, 8781, and 8784. The intent of the design update is to reduce the potential for tissue growth into the Ascenda catheter…
Class IIFDA: OngoingMedtronic Neuromodulation
Medical DeviceJul 24, 2024
Medical Depot Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury recall — FDA Z-2354-2024
The tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustain an injury
Class IIFDA: OngoingMedical Depot Inc.
Medical DeviceJul 24, 2024
Hologic Horizon X-Ray Bone Densitometer (DXA) Models: Horizon-A, Horizon-W, Horizon-WI recall — FDA Z-2373-2024
Non-conformance pertains to electromagnetic compatibility requirements according to the international technical standard IEC 60601-1-2 for the safety and essential performance of medical…
Class IIFDA: OngoingHologic Inc.
Medical DeviceJul 24, 2024
Becton, Dickinson and Company, BD Biosciences BD Multitest 6-Color TBNK CE-IVD, REF: 644611 recall — FDA Z-2351-2024
Multitest with compromised raw material used to assess immune system status may result in flow cytometry plot with unusual staining pattern, nonspecific aggregates, high background, double…
Class IIFDA: OngoingBecton, Dickinson and Company, BD Biosciences
Medical DeviceJul 24, 2024
B. Braun Medical OUTLOOK IV SET 15DROP W/3 CARESITE-Used with an electrically-powered recall — FDA Z-2377-2024
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime,…
Class IIFDA: OngoingB. Braun Medical, Inc.
Medical DeviceJul 24, 2024
B. Braun Medical Infusomat UNIV. 15 DROP PUMP SET W/2 CARESITE CV- Used with an recall — FDA Z-2399-2024
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime,…
Class IIFDA: OngoingB. Braun Medical, Inc.
Medical DeviceJul 24, 2024
B. Braun Medical Infusomat UNIV. 15 DR PUMP SET, 1.2 FIL, 2 CRSITE-Used with an recall — FDA Z-2379-2024
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime,…
Class IIFDA: OngoingB. Braun Medical, Inc.
Medical DeviceJul 24, 2024
B. Braun Medical Infusomat SPACE PUMP IV SET 15D, 90 IN recall — FDA Z-2396-2024
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime,…
Class IIFDA: OngoingB. Braun Medical, Inc.
Medical DeviceJul 24, 2024
Abbott Proclaim 7 Implantable Pulse Generator, REF 3663, Sterile EO, Rx Only recall — FDA Z-2361-2024
The duration between the implantable pulse generator reaching the elective replacement indicator threshold and end of service may be shorter than indicated in product labeling.
Class IIFDA: OngoingAbbott Medical
Medical DeviceJul 24, 2024
MED-EL Elektromedizinische Gereate, Gmbh Mi1250 SYNCHRONY 2, Item Numbers: a) 39541 recall — FDA Z-2356-2024
A small number of devices may have a higher probability of a crack within the internal electronics substrate which could result in a non-functional device.
Class IIFDA: OngoingMED-EL Elektromedizinische Gereate, Gmbh
Medical DeviceJul 24, 2024
B. Braun Medical Infusomat UNIV. 15 DROP PUMP SET, 3 ULTRASITE, ASV-Used with an recall — FDA Z-2403-2024
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime,…
Class IIFDA: OngoingB. Braun Medical, Inc.
Medical DeviceJul 24, 2024
B. Braun Medical Infusomat UNIV.15DROP PUMP SET W/3 SAFELINE LL-Used with an recall — FDA Z-2378-2024
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime,…
Class IIFDA: OngoingB. Braun Medical, Inc.
Medical DeviceJul 24, 2024
B. Braun Medical Infusomat UNIV 60 DROP PUMP SET, W/2 CARESITE INJ. -Used with an recall — FDA Z-2401-2024
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime,…
Class IIFDA: OngoingB. Braun Medical, Inc.
Medical DeviceJul 24, 2024
B. Braun Medical Infusomat SPACE PUMP IV SET 15D, 110 IN. -Used with an electrically-powered recall — FDA Z-2394-2024
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime,…
Class IIFDA: OngoingB. Braun Medical, Inc.
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September 2026364 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categories